еКорпус – библиографски запис
Ameloblastic fibroma: a rare case report with 7-year follow-up
Амелобластни фибром: приказ ретког случаја са седмогодишњим периодом клиничког праћења
- Часопис
- Serbian Archives of Medicine
- Објављено
- Srp Arh Celok Lek. 2015;143(3–4):190–194.
- Врста рада
- CASE REPORTS
Abstract
Introduction Ameloblastic fibroma (AF) is a rare benign odontogenic tumor that usually occurs in the first two decades of life. It affects adolescents and young adults and is found in the mandible and with a higher frequency in the posterior region of this segment. There are rare case reports with a long-term follow-up.
Case Outline We report the case of a 6-year-old boy with extensive ameloblastic fibroma in the mandible. Treatment consisted of enucleation and bone curettage, with the preservation of permanent teeth adjacent to the tumor. Clinical and radiographic follow-up of the patient over a period of 7 years showed no signs of recurrence or malignant transformation.
Conclusion Patients with AF should be under follow-up for prolonged periods of time, even in cases exhibiting a low proliferation index, because of the potential for recurrence and malignant transformation of this tumor.
Keywords: ameloblastic fibroma; odontogenic tumors; jaws; follow-up